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Volume 18, Number 10—October 2012

Research

Constant Transmission Properties of Variant Creutzfeldt-Jakob Disease in 5 Countries

Abigail B. Diack, Diane Ritchie, Matthew Bishop, Victoria Pinion, Jean-Philippe Brandel, Stephane Haik, Fabrizio Tagliavini, Cornelia Van Duijn, Ermias D. Belay, Pierluigi Gambetti, Lawrence B. Schonberger, Pedro Piccardo, Robert G. Will1, and Jean C. Manson1Comments to Author 
Author affiliations: The Roslin Institute, Easter Bush, Scotland, UK (A.B. Diack, V. Pinion, J.C. Manson); University of Edinburgh, Edinburgh, Scotland, UK (D. Ritchie, M. Bishop, R.G. Will); Cellule Nationale de Référence des Maladies de Creutzfeldt-Jakob, Universite Pierre et Marie Curie-Paris 6, INSERM, and CNRS, Paris, France (J.-P. Brandel, S. Haik); Fdazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy (F. Tagliavini); Erasmus University Medical School, Rotterdam, the Netherlands (C. Van Duijn); Centers for Disease Control and Prevention, Atlanta, Georgia, USA (E.D. Belay, L.B. Schonberger); Case Western Reserve University, Cleveland, Ohio, USA (P. Gambetti); and Food and Drug Administration, Rockville, Maryland, USA (P. Piccardo)

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Figure 3

Immunohistochemical detection of abnormal prion protein (PrPSc) in the hippocampus and thalamus of RIII, C57, and VM wild-type mice after inoculation with variant Creutzfeldt-Jakob disease brain tissue. Scale bars = 500 µm. The anti–prion protein detection antibody used was 6H4.

Figure 3. . Immunohistochemical detection of abnormal prion protein (PrPSc) in the hippocampus and thalamus of RIII, C57, and VM wild-type mice after inoculation with variant Creutzfeldt-Jakob disease brain tissue. Scale bars = 500 µm. The anti–prion protein detection antibody used was 6H4.

Main Article

1Joint senior authors.

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